Proteolipid protein gene: Pelizaeus–Merzbacher disease in humans and neurodegeneration in mice-Reference-Cited by-同舟云学术

Proteolipid protein gene: Pelizaeus–Merzbacher disease in humans and neurodegeneration in mice

Published:1999-04 Issue:4 Volume:15 Page:125-128
ISSN:0168-9525
Container-title:Trends in Genetics
language:en
Short-container-title:Trends in Genetics

Author:

Woodward Karen,Malcolm Sue

Publisher

Elsevier BV

Subject

Genetics

Reference31 articles.

1. Eine eigenartige familiäre-hereditäre Erkrankungsform (Aplasia axialis extracorticalis congenita);Merzbacher;Z. Ges. Neurol. Psychiatr.,1910

2. Seitelberger, F. (1970) Pelizaeus–Merzbacher disease, in Handbook of Clinical Neurology. Leucodystrophies and Poliodystrophies (Vol. 42) (Vinken, P.J. and Bruyn, G.W., eds), 150–202, North-Holland

3. X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus;Saugier-Veber;Nat. Genet.,1994

4. Charcot-Marie-Tooth disease: lessons in genetic mechanisms;Lupski;Mol. Med.,1998

5. Proteolipid protein gene dosage effect in Pelizaeus–Merzbacher disease;Ellis;Nat. Genet.,1994

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